"V体育2025版" Evaluation of asthma-chronic obstructive pulmonary disease overlap using a mouse model of pulmonary disease
- PMID: 36474247
- PMCID: V体育官网 - PMC9728005
- DOI: 10.1186/s12950-022-00322-x
Evaluation of asthma-chronic obstructive pulmonary disease overlap using a mouse model of pulmonary disease
"V体育官网入口" Erratum in
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Correction: Evaluation of asthma-chronic obstructive pulmonary disease overlap using a mouse model of pulmonary disease.J Inflamm (Lond). 2023 Jan 20;20(1):3. doi: 10.1186/s12950-023-00326-1. J Inflamm (Lond). 2023. PMID: 36670416 Free PMC article. No abstract available.
Abstract
Background: Features of asthma and chronic obstructive pulmonary disease (COPD) can coexist in the same patient, in a condition termed asthma- chronic obstructive pulmonary disease overlap (ACO). ACO is heterogeneous condition exhibiting various combinations of asthma and COPD features. No clinically acceptable experimental model of ACO has been established. We aimed to establish an animal model of ACO. VSports手机版.
Methods: We generated two phenotypes of ACO by administering ovalbumin and porcine pancreatic elastase in combination, and papain. The proinflammatory cytokines and cell types in bronchoalveolar lavage fluid (BALF) were investigated, and lung function parameters were measured using the FlexiVent system V体育安卓版. .
Results: Greater airway inflammation was observed in the asthma and both ACO models, and emphysema was found in the COPD and both ACO models V体育ios版. The proportion of eosinophils in BALF was elevated in the asthma and ACO-a model. Type 2 inflammatory cytokine levels were highest in the ACO-a model, and the neutrophil gelatinase-associated lipocalin level was elevated in the asthma and ACO-a model. Of lung function parameters, compliance was greater in the COPD and ACO-b model, in which elastance was lower than in the asthma model. Airway resistance increased with the methacholine concentration in the asthma and both ACO models, but not in the control or COPD model. .
Conclusion: We established two murine models of ACO that exhibit features of asthma and COPD. We validated the clinical relevance of the ACO models based on changes in cytokine profiles and lung function VSports最新版本. These models will be useful in further studies of the pathogenesis of, and therapeutic targets for ACO. .
Keywords: Asthma; Chronic obstructive pulmonary disease; Cytokine; Experimental model; Lung function. V体育平台登录.
© 2022. The Author(s).
Conflict of interest statement (V体育官网)
The authors have no potential conflict of interest relevant to this article.
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References
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- Global Initiative for Asthma. Global Strategy for Asthma Management and Prevention: 2021 Update. (2022). Available online at: V体育2025版 - http://www.ginasthma.org (accessed 15 May 2022). [Internet].
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- Global Initiative for Chronic Obstructive Lung Disease. Global Strategy for the Diagnosis, Management, and Prevention of Chronic Obstructive Pulmonary Disease: 2022 Update. Available online: http://www.goldcopd.org (accessed on 15 May 2022). [Internet].
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